DMPK

Nurix•Brisbane, CA

4d•$92,891 - $124,079•Onsite

About The Position

Nurix Therapeutics is searching for a motivated Research Associate to join our Bioanalytical-In Vitro DMPK team. The successful candidate will contribute to the bioanalytical efforts to support Nurix drug discovery programs involving in vivo and in vitro studies. We are seeking a highly motivated research associate to characterize the in vitro and in vivo ADME properties of drug candidates. The primary responsibilities will be to conduct bioanalysis for in vivo samples and to conduct in vitro experiments. The scope of the daily responsibilities for this position includes, but is not limited to, developing bioanalytical methods, quantitating drug candidates and their metabolites, endogenous biomarkers in biological matrices (e.g. blood, plasma, tissue, tumor, CSF, etc.), reporting bioanalytical results and managing projects outsourced in CROs to support all in vitro and in vivo studies. The successful candidate will have extensive experience in bioanalytical method development and sample analysis using LC-MS/MS and other analytical techniques.

Requirements

BS or master’s with >4 years’ experience working in a discovery setting using LC-MS/MS within a pharmaceutical/biotechnology company
Broad experience in small molecule drug candidate bioanalytical assay development/sample analysis in different biological matrices using LC-MS/MS
Experience with AB SCIEX mass spectrometry software
Excellent written, verbal communications and interpersonal skills to collaborate with internal and external partners in a matrix environment

Nice To Haves

Experience with H/UPLC and mass spectrometry
Good working knowledge of SCIEX LC-MS/MS systems for small molecule quantitation
PK analysis using Phoenix or other data management software
Management experience with CROs for outsourcing BA activities is preferred
Provide sample analysis to support PK, PK/PD, PK/efficacy, distribution, metabolism, and non-GLP toxicology studies
Identify issues and troubleshoot scientific equipment including LC-MS/MS, select and develop appropriate methods to perform experiments, analyze data and prepare related reports.
Excellent oral and written communication skills

Responsibilities

Provide bioanalytical support for in-house PK, non-GLP safety TK
Conduct bioanalytical method development and qualification to support drug, metabolite and biomarker analysis
Independently develop LC-MS/MS methods to quantitate small molecules in in vitro and in vivo samples
Conduct in-vitro stability assays to understand metabolism of drugs
Perform metabolic identification (MetID) using LC-QTOF MS/MS, including accurate mass analysis, fragment interpretation and biotransformation pathway assignment
Independently operate, troubleshoot and maintain LC-MS/MS systems
Participate in multidisciplinary project teams and collaborate with other departments to understand bioanalytical needs for both PK and PD support
Manage projects conducted at CROs to ensure high quality bioanalytical data is delivered to meet project timelines
Maintain accurate and detailed scientific electronic laboratory notebooks
Perform all duties in keeping with the Company’s core values, policies and all applicable regulations